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Efficacy of Minimally Invasive Surgical Technique in Accelerating Orthodontic Treatment

Evaluation the Efficacy of Flapless Corticotomy Accomplished by Either Hard-laser or Piezosurgey in Accelerating Upper Canine Retraction and Evaluation of the Dento-alveolar Changes and the Levels of Acceptance and Discomfort.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02606331
Enrollment
36
Registered
2015-11-17
Start date
2015-04-30
Completion date
2016-06-30
Last updated
2016-06-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malocclusion, Angle Class II

Brief summary

Thirty six patients needs therapeutic extraction of the maxillary first premolars with subsequent retraction of the maxillary canines will be divided randomly into two groups : piezocision group and the ER:yttrium aluminum garnet (YAG) laser group. In each group, piezocision or hard laser-assisted flapless corticotomy will randomly assigned to one side of the maxillary arch at the first premolar region, and the other side served as the control. Canine retraction will be initiated after completion of the leveling and alignment phase via closed nickel-titanium coil springs applying 150 g of force per side, soldered trans-palatal arch will be used as an anchor unit. Pre- and post distalization dental casts will be evaluated to study rate of canine distalization, canine rotation and anchorage loss over a follow-up period until a Class I canine relationship is achieved. The levels of pain and discomfort will be self-reported using a questionnaire with visual analog scales administered at four assessment times during the first month after the minimally invasive procedure.

Detailed description

One main issue in orthodontics is the prolonged treatment time, leading patients, especially adults, to avoid treatment or seek alternative options such as implants or veneers with less than optimal results. Therefore, the search for methods that decrease the treatment duration is a main challenge in orthodontic research. Decreased duration of therapy seems to be related not only to better patient compliance, but also to reduced treatment -related root resorption , better periodontal health and lower risk of caries and white spots. Adjunct to the proper selection of brackets, wires, biomechanic systems, force levels, and anchorage systems, an array of novel techniques has been introduced to accelerate orthodontic tooth movement. These techniques can be briefly categorized as surgical and non-surgical. However The surgical approach is the most clinically used and most tested with known predictions and stable results. The invasiveness of surgical procedures, requiring full mucoperiosteal flaps, might have been a drawback for their widespread acceptance among orthodontists and patients. Therefore, more conservative flapless corticotomy techniques have recently been proposed. Although various techniques of flapless corticotomy have been reported to be successful in practice, scientific evidence for their effectiveness so far has been limited to case series and a handful of clinical trials, generally with small groups. Therefore further controlled prospective studies are needed to study the effectiveness of flapless corticotomy in accelerating orthodontic tooth movement .

Interventions

PROCEDUREPiezosurgery

Corticotomy cuts will be performed by this technique.

RADIATIONER:YAG laser

Corticotomy cuts will be performed by this technique.

Sponsors

Damascus University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
14 Years to 27 Years
Healthy volunteers
No

Inclusion criteria

* Adult healthy patients , Male and female , Age range: 15-27 years. * Class II Division 1 malocclusion : * Mild / moderate skeletal Class II (sagittal discrepancy angle ≤7) * Overjet ≤10 * Normal or excessive facial height (Clinically and then cephalometrically assessed using these three angles : mandibular/cranial base angle, maxillary/mandibular plane angle and facial axis angle) * Mild to moderate crowding ≤ 4 * Permanent occlusion. * Existence of all the upper teeth (except third molars). * Good oral and periodontal health: * Probing depth \< 4 mm * No radiographic evidence of bone loss . * Gingival index ≤ 1 * Plaque index ≤ 1

Exclusion criteria

* Medical problems that affect tooth movement (corticosteroid, nonsteroidal antiinflammatory drugs (NSAIDs), …) * patients have anti indication for oral surgery ( medical - social - psycho) * Presence of primary teeth in the maxillary arch * Missing permanent maxillary teeth (except third molars). * Poor oral hygiene or Current periodontal disease: * Probing depth ≥ 4 mm * radiographic evidence of bone loss * Gingival index \> 1 * Plaque index \> 1 * Patient had previous orthodontic treatment

Design outcomes

Primary

MeasureTime frameDescription
Rate of canine retractionThis will be measured immediately at the end of the tooth movement, i.e. when the retracted canine reaches its final position which takes up to 12 weeksThe distance traveled by mm is divided by the time required in weeks.

Secondary

MeasureTime frameDescription
Rate of molar anchorage lossThis will be measured immediately at the end of the tooth movement, i.e. when the retracted canine reaches its final position which may take up to 12 weeksThe amount of mesial movement of the first molar in millimeters (mm) is divided by the time required to retract the upper canines (in weeks).
Change in canine rotationThis will be measured at the following assessment times: T1: baseline, T2: after 4 weeks of canine retraction, T3: after 8 weeks of canine retraction, T4: when the canine reaches its final position up to 12 weeksThis measurement will be performed on plaster models taken at the aforementioned assessment times.
Change in the levels of pain and discomfortThese levels will be assessed at: one day following the intervention, one week, two weeks, and four weeks following the intervention.Assessment will be performed using questionnaires via visual analog scales.

Countries

Syria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026